Galizio M, Perone M
J Exp Anal Behav. 1987 Jan;47(1):115-26. doi: 10.1901/jeab.1987.47-115.
Rats were trained on concurrent schedules in which pressing one lever postponed shock and pressing the other occasionally (variable-interval schedule) produced a 2-min timeout during which the shock-postponement schedule was suspended and its correlated stimuli were removed. These procedures provided a baseline for studying the effects of drugs on behavior maintained by different sources of negative reinforcement (shock avoidance and timeout from avoidance). Experiment 1 studied a benzodiazepine agonist, chlordiazepoxide, and antagonist, CGS 8216. Chlordiazepoxide (2.5-30 mg/kg) had little effect on avoidance responding except at higher doses, when it reduced responding. By comparison, responding on the timeout lever was increased in 5 of 6 rats. These effects were reversed by CGS 8216 (2.5-5 mg/kg) in the 2 rats tested, but CGS 8216 had no effect by itself. Experiment 2 studied an opiate agonist, morphine, and antagonist, naltrexone, with 3 rats. Morphine's (2.5-20 mg/kg) effects were opposite those of chlordiazepoxide: At doses that either increased or had no effect on avoidance responding, morphine depressed timeout responding. Naltrexone (5 mg/kg) reversed these actions but had no effect by itself.
对大鼠进行并发程序训练,按压一个杠杆可推迟电击,按压另一个杠杆(可变间隔程序)偶尔会产生2分钟的暂停期,在此期间电击推迟程序暂停,其相关刺激被移除。这些程序为研究药物对由不同负强化源(避免电击和避免后的暂停)维持的行为的影响提供了基线。实验1研究了苯二氮䓬类激动剂氯氮卓和拮抗剂CGS 8216。氯氮卓(2.5 - 30毫克/千克)对回避反应影响不大,除非剂量较高时会减少反应。相比之下,6只大鼠中有5只在暂停杠杆上的反应增加。在测试的2只大鼠中,CGS 8216(2.5 - 5毫克/千克)逆转了这些效应,但CGS 8216本身没有作用。实验2用3只大鼠研究了阿片类激动剂吗啡和拮抗剂纳曲酮。吗啡(2.5 - 20毫克/千克)的作用与氯氮卓相反:在对回避反应增加或无影响的剂量下,吗啡抑制暂停反应。纳曲酮(5毫克/千克)逆转了这些作用,但本身没有作用。